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Catalog Number:
41321
CAS Number:
57288-03-6
( S )-(-)-Aminoglutéthimide
Purity:
≥ 97 % (dosage)
Synonym(s):
( S )-3-(4-aminophényl)-3-éthylpipéridine-2,6-dione, (3 S )-3-Amino-4-éthyl-4-phénylpipéridine-2,6-dione
Documents
$194.99 /500 mg
Taille
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Informations sur le produit

(S)-(-)-Aminoglutethimide is a chiral compound recognized for its significant role in pharmaceutical applications, particularly in the treatment of hormone-dependent cancers. This compound acts as an aromatase inhibitor, effectively reducing estrogen levels in the body, which is crucial for managing conditions such as breast cancer. Its unique structure allows it to selectively target specific pathways, making it a valuable tool in both research and clinical settings.

In addition to its therapeutic uses, (S)-(-)-Aminoglutethimide has been explored in various studies for its potential in endocrine therapies and as a precursor in the synthesis of other bioactive compounds. Researchers appreciate its ability to facilitate the development of innovative treatments, providing a foundation for further advancements in cancer therapy. With its proven efficacy and versatility, (S)-(-)-Aminoglutethimide stands out as a compound of choice for professionals in the pharmaceutical and research industries.

Numéro CAS 
57288-03-6
Formule moléculaire
C13H16N2O2
Poids moléculaire 
232.28
Point de fusion 
115,5 - 119,5 °C (lit.)
Rotation optique 
[α] 20 D = -160 ± 2 ° (C = 1 dans MeOH)
Informations générales
Numéro CAS 
57288-03-6
Formule moléculaire
C13H16N2O2
Poids moléculaire 
232.28
Point de fusion 
115,5 - 119,5 °C (lit.)
Rotation optique 
[α] 20 D = -160 ± 2 ° (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(S)-(-)-Aminoglutethimide is widely utilized in research focused on

  • Pharmaceutical Development: This compound is primarily used in the synthesis of various pharmaceuticals, particularly in the development of medications for hormone-related conditions, such as adrenal tumors.
  • Cancer Research: It plays a role in studies aimed at understanding and treating certain types of cancer, especially those influenced by steroid hormones, providing insights into potential therapeutic pathways.
  • Endocrinology: Researchers leverage its properties to investigate adrenal function and disorders, aiding in the development of treatments for conditions like Cushing's syndrome.
  • Analytical Chemistry: The compound is utilized in analytical methods to quantify steroid hormones in biological samples, enhancing the accuracy of diagnostic tests.
  • Drug Interaction Studies: It serves as a valuable tool in pharmacokinetic studies, helping scientists understand how different drugs interact within the body, which is crucial for safe medication development.

Citations